[Press the ” > ” button above and turn up your volume.]
Listen to Dr Lynch discuss his recent findings of how his entire family has MTHFR mutations – and some severe forms.
How is that the path we take in life is somehow absolutely appropriate and fitting for us?
Becoming a naturopathic physician with a specialty in environmental medicine and nutrigenomics, I am stunned at how critical this path was for me – and for my family.
If I had not chosen this path, two of my boys would most likely be quite autistic, my wife would be suffering from rheumatoid arthritis and my health would have been severely compromised.
As one who has spent a lot of time with MTHFR research and working with countless clients with MTHFR, I can safely say I am quite well-versed in MTHFR mutations.
I was waiting until my new comprehensive genetic test was nearly completed before I tested myself and my family for MTHFR.
As I nervously opened the PDF documents for each member of my family, I was blown away. (I am glad I was on vacation when I opened these documents.)
- Theodor Lynch, Male, Age 3: Homozygous A1298C
- Mathew Lynch, Male, Age 6: Heterozygous A1298C + Heterozygous C677T
- Tasman Lynch, Male, Age 9, Heterozygous A1298C
- Nadia Lynch, Female, Age 35, Heterozygous A1298C
- Benjamin Lynch, Male, Age 38, Heterozygous A1298C + Heterozygous C677T
My mindset totally shifted from simply being a father to suddenly being my childrens’ guide and physician. Without my assistance, their future is grim.
Yes. Those were the exact words when I saw Theodor’s and Mathew’s test results.
A million concerns ran through my head wondering what I should do.
Then, I realized something.
“I’m already doing something for them – many ‘somethings’.”
- Gluten Free Diet
- Dairy Free Diet
- Sauna for whole family at least 20 times a year
- Filtered water
- No carpets in the house
- Air purification
- Organic food
- Very limited processed foods
- No artificial soaps, odors, perfumes
- No cleaning solutions – just natural soaps, vinegar
- Limited pressboard in our home
- Organic bedding and mattresses
- Multivitamin with methylfolate, pure fish oil, CoQ10, Cal/Mag, vitamin D3
- Limited sugar intake
- No soda
- Highly active in sports and outdoors for all of us
- Studying piano
- Speaking and learning Russian
All of these are critical to treating MTHFR mutations.
Many doctors typically tell their patients with newly diagnosed MTHFR mutations:
- “Take 5 mg of folic acid a day and you’ll be fine.”
- “MTHFR is nothing to worry about.”
- “Take 1 x 15 mg Deplin daily and you’ll be great.”
- “Take NeevoDHA while pregnant along with Lovenox and all will be great.”
All of these recommendations are wrong – in my opinion.
If you are not doing 1 through 16 above, then you are not fully addressing your MTHFR mutation.
Let me give you some more background:
Both Mathew and Theo were slow to speak yet are quite healthy overall.
Mathew’s speech is now fantastic yet he has an accent – I believe this comes from his mother’s thick Russian accent. She was his one and only person to interact with – well – besides his older brother. I was not around in his younger years (medical school is extremely demanding for 5 years). Then add on the fact that Mathew was not in an English speaking daycare/preschool until later.
Slow speech can be attributed to a few things in Mathew’s and Theo’s life:
- We’re a bilingual family: Russian and English
- Summers spent in Russia during critical language development (no English spoken).
- MTHFR, PEMT and GAMT mutations
- Me having been in medical school and not around much to interact with my children.
- Not starting an English preschool or interaction with many other English speaking children until later – age 5 for Mathew. Theodor is in Russian preschool now.
I smiled when I saw my wife’s MTHFR results.
I test her for everything and she nearly always comes back squeaky clean yet she suffered terribly with Rheumatoid Arthritis from the young age of 17 until 31.
She now is literally ‘normal’ and living life without rheumatoid arthritis.
Lifestyle, diet and supplements.
“Is that right?”
These were the words I internally said to myself as I stared at the lab report for Benjamin Lynch.
1 copy of A1298C and 1 copy of C677T
I was amazingly calm but confused.
How come I am not showing more symptoms?
I used to – in a big way.
- Chronic fatigue
- Chemically sensitive
- Skin rashes
- Always low WBC levels
I now follow points 1 to 17 on the above list and have been for years. This is why I show no symptoms.
In a nutshell:
MTHFR mutations do not control you. You control them.
I, and my family, are living proof that you can beat MTHFR mutations through proper lifestyle, diet and supplementation – and mindset.
How much methylfolate are we all taking?
None of us are taking more than 400 mcg a day currently.
MTHFR is not about methylfolate.
MTHFR mutations demand a healthy lifestyle and some methylfolate.
There is no pill for MTHFR.
There is no surgery for MTHFR.
What there is for MTHFR is work and awareness.
If you respect what you put into your body and what is around it, you’ll lead a healthy life.
Now – it is not always this easy.
Because there are other potential mutations which increase the severity of the MTHFR mutation.
COMT, VDR, CBS, MTR/MTRR, BHMT, MAO A, DHPR, SUOX, SOD, GST, NOS – to name a few.
Main point I want to leave you with though is you control your genetics.
They do not control you.
See Theo celebrate!!
He doesn’t care he has the MTHFR A1298C homozygous variant!!! 🙂